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HRID 1157384作成日:2026年10月27日

Cesium carbonate → Tert-butyl N-[(4-cyanophenyl)methyl]-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamate

https://huagongshe.com/reaction/1157384

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-(Bromomethyl)benzonitrileHCID 86996—
反応物Di-tert-butyl IminodicarboxylateHCID 279800—
触媒Lithium iodideHCID 66321—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl N-[(4-cyanophenyl)methyl]-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamateHCID 368376883.4%

反応条件

温度70 °C

反応手順

4-(Bromomethyl)benzonitrile (5 g, 25.5 mmoles) and di-tert-butyliminodicarboxylate (5.54 g, 25.5 mmoles) were dissolved in anhydrous THF (50 mL) and cesium carbonate (16.62 g, 25.5 mmoles) and lithium iodide (170.5 mg, 1.275 mmoles) were added. The mixture was stirred at 70° C. for 23 h and the reaction was worked up as described in Preparative Example 244, Step B above. The residue was chromatographed on a silica gel column (50×5 cm) using 5% ethyl acetate in hexane as the eluant to give 4-(di-tert-butoxycarbonylaminomethyl)benzonitrile (7.07 g, 83%): FABMS: m/z 333.2 (MH+); HRFABMS: m/z 333.1816 (MH+). Calcd. for C18H25N2O4: m/z 333.1814; δH (CDCl3) 1.45 (18H, s, —COOC(CH3)3), 4.81 (2H, s, CH2), 7.37 (2H, d, Ar—H) and 7.62 ppm (2H, d, Ar—H); δC (CDCl3) CH3, 28.1, 28.1, 28.1, 28.1, 28.1, 28.1; CH2, 49.2; CH, 127.8, 127.8, 132.3, 132.3; C, 83.2, 83.2, 111.1, 118.9, 144.1, 152.4, 152.4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07807683B2
出典データセットuspto-grants-2010_10
ORD IDord-342e233134ed4d429609eaf3d2ee1b9f
出典メモuspto-grants-2010_10